A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431693



Internal ID22489563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117371293..117373262hg38UCSC Ensembl
chr7:117011347..117013316hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg381970
hg191970
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971929
Supporting Variants
Samples
Known GenesASZ1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431693
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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